메뉴 건너뛰기




Volumn 65, Issue 47, 2009, Pages 9713-9718

Tryst with a molecular and supramolecular oddity: an anti-Fürst-Plattner epoxide opening product as a designer additive for accessing an elusive polymorph

Author keywords

Crystal engineering; Hydrogen bonds; Hydrolysis; Polycyclitols; Polymorphism

Indexed keywords

ACETIC ACID DERIVATIVE; DIMORPHECOLIC ACID; DRUG ADDITIVE; EPOXIDE; ESTER DERIVATIVE; HYDROGEN; OXYGEN;

EID: 70349972665     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.09.092     Document Type: Article
Times cited : (8)

References (63)
  • 12
    • 70349950162 scopus 로고    scopus 로고
    • Over the recent years, a lot of attention has been focused on analyzing, through experimental, theoretical and statistical techniques, the influence that competition between intra- and intermolecular hydrogen bonding might have on the physical and chemical behavior of molecules in gas, liquid or solid phase. Indeed, this subtle interplay goes a long way in determining a number of molecular properties such as the preferred conformation, solubility, acidity and electrochemical behaviour. For recent reports, see
    • Over the recent years, a lot of attention has been focused on analyzing, through experimental, theoretical and statistical techniques, the influence that competition between intra- and intermolecular hydrogen bonding might have on the physical and chemical behavior of molecules in gas, liquid or solid phase. Indeed, this subtle interplay goes a long way in determining a number of molecular properties such as the preferred conformation, solubility, acidity and electrochemical behaviour. For recent reports, see:
  • 25
    • 19744382026 scopus 로고    scopus 로고
    • also see the special issue on polymorphism in
    • also see the special issue on polymorphism in. Cryst. Growth Des. 4 (2004) 1085-1444
    • (2004) Cryst. Growth Des. , vol.4 , pp. 1085-1444
  • 27
    • 0002236599 scopus 로고
    • Papers Int. Congr. Pure Appl. Chem., 12th, New York, NY
    • Fürst, A.; Plattner, P. A. Abstr. Papers Int. Congr. Pure Appl. Chem., 12th, New York, NY, 1951; 409.
    • (1951) , pp. 409
    • Fürst, A.1    Plattner, P.A.A.2
  • 28
    • 70349937519 scopus 로고    scopus 로고
    • For examples of anti-Fürst-Plattner opening of epoxides, see
    • For examples of anti-Fürst-Plattner opening of epoxides, see:
  • 35
    • 70349928250 scopus 로고    scopus 로고
    • For references on the control of crystal polymorphism via the use of tailor-made nucleation inhibitors, see
    • For references on the control of crystal polymorphism via the use of tailor-made nucleation inhibitors, see:
  • 41
  • 45
    • 70349943423 scopus 로고    scopus 로고
    • note
    • α radiation on a Philips PANalytical X′Pert PRO MPD diffractometer, operating at 40 kV and 30 mA.
  • 46
    • 26744461416 scopus 로고
    • Molecules, possessing a center of symmetry, usually crystallize in centrosymmetric space groups and tend to occupy a crystallographic inversion center; see
    • Molecules, possessing a center of symmetry, usually crystallize in centrosymmetric space groups and tend to occupy a crystallographic inversion center; see. Brock C.P., and Dunitz J.D. Chem. Mater. 6 (1994) 1118-1127
    • (1994) Chem. Mater. , vol.6 , pp. 1118-1127
    • Brock, C.P.1    Dunitz, J.D.2
  • 48
    • 70349957645 scopus 로고    scopus 로고
    • For recent reports on additive induced polymorphism, see
    • For recent reports on additive induced polymorphism, see:
  • 50
  • 55
    • 0004283942 scopus 로고    scopus 로고
    • University of Göttingen, Germany
    • Sheldrick G.M. SADABS (1996), University of Göttingen, Germany
    • (1996) SADABS
    • Sheldrick, G.M.1
  • 57
    • 0004150157 scopus 로고    scopus 로고
    • University of Göttingen, Germany
    • Sheldrick G.M. SHELXL97 (1997), University of Göttingen, Germany
    • (1997) SHELXL97
    • Sheldrick, G.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.